<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hu Y</submitter><funding>Fundamental Research Funds for Central Universities of the Central South University</funding><funding>National Natural Science Foundation of China</funding><pagination>48-56</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8690181</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>The one-pot synthesis of methyl isobutyl ketone (MIBK) and methyl isobutyl methanol (MIBC) from acetone and hydrogen is a typical cascade reaction comprised of aldol condensation-dehydration-hydrogenation. Pd loss and aggregation during long term operation are typical problems in industrial application. In this paper, an active and stable catalyst was achieved with defective UiO-66 as a support for Pd, which was synthesized with the ratio 15 : 1 of ZrOCl&lt;sub>2&lt;/sub>·8H&lt;sub>2&lt;/sub>O to ZrCl&lt;sub>4&lt;/sub> as Zr-precursors. The resultant Pd catalyst remained active for at least 1000 h with a MIBK + MIBC selectivity of 84.87-93.09% and acetone conversion of 45.26-53.22% in a continuous trickle-bed reactor. Besides the increased Brønsted acid amount generated by the defect sites was favorable for the activity, the cavity confinement in the UiO-66 (&lt;i>R&lt;/i> = 15 : 1) structure also efficiently prevented Pd loss and aggregation during the long term run. The contrast of the characterization of the fresh and used Pd/UiO-66 (&lt;i>R&lt;/i> = 15 : 1) indicated that the deactivation of the catalyst was attributed to carbonaceous accumulation on the catalyst surface, which could be easily regenerated by calcination. This work supplied a new alternative for the design and utilization of industrial catalysts for MIBK and MIBC synthesis.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>An active and stable multifunctional catalyst with defective UiO-66 as a support for Pd over the continuous catalytic conversion of acetone and hydrogen.</pubmed_title><pmcid>PMC8690181</pmcid><funding_grant_id>21676303</funding_grant_id><funding_grant_id>2020zzts415</funding_grant_id><pubmed_authors>Lin B</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Mei Y</pubmed_authors><pubmed_authors>Du X</pubmed_authors><pubmed_authors>Xu F</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Wang K</pubmed_authors></additional><is_claimable>false</is_claimable><name>An active and stable multifunctional catalyst with defective UiO-66 as a support for Pd over the continuous catalytic conversion of acetone and hydrogen.</name><description>The one-pot synthesis of methyl isobutyl ketone (MIBK) and methyl isobutyl methanol (MIBC) from acetone and hydrogen is a typical cascade reaction comprised of aldol condensation-dehydration-hydrogenation. Pd loss and aggregation during long term operation are typical problems in industrial application. In this paper, an active and stable catalyst was achieved with defective UiO-66 as a support for Pd, which was synthesized with the ratio 15 : 1 of ZrOCl&lt;sub>2&lt;/sub>·8H&lt;sub>2&lt;/sub>O to ZrCl&lt;sub>4&lt;/sub> as Zr-precursors. The resultant Pd catalyst remained active for at least 1000 h with a MIBK + MIBC selectivity of 84.87-93.09% and acetone conversion of 45.26-53.22% in a continuous trickle-bed reactor. Besides the increased Brønsted acid amount generated by the defect sites was favorable for the activity, the cavity confinement in the UiO-66 (&lt;i>R&lt;/i> = 15 : 1) structure also efficiently prevented Pd loss and aggregation during the long term run. The contrast of the characterization of the fresh and used Pd/UiO-66 (&lt;i>R&lt;/i> = 15 : 1) indicated that the deactivation of the catalyst was attributed to carbonaceous accumulation on the catalyst surface, which could be easily regenerated by calcination. This work supplied a new alternative for the design and utilization of industrial catalysts for MIBK and MIBC synthesis.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-05T13:07:51.626Z</modification><creation>2025-04-05T13:07:51.626Z</creation></dates><accession>S-EPMC8690181</accession><cross_references><pubmed>35423013</pubmed><doi>10.1039/d0ra09217g</doi></cross_references></HashMap>